Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
  • A61K47/02—Inorganic compounds
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
  • A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
  • A61K47/36—Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
  • A61K47/38—Cellulose; Derivatives thereof
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
  • A61K8/27—Zinc; Compounds thereof
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
  • A61K8/29—Titanium; Compounds thereof
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
  • A61K8/73—Polysaccharides
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K9/00—Medicinal preparations characterised by special physical form
  • A61K9/06—Ointments; Bases therefor; Other semi-solid forms, e.g. creams, sticks, gels
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
  • A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
  • B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
  • B05D1/00—Processes for applying liquids or other fluent materials
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
  • C08B1/00—Preparatory treatment of cellulose for making derivatives thereof, e.g. pre-treatment, pre-soaking, activation
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
  • C08B11/00—Preparation of cellulose ethers
  • C08B11/02—Alkyl or cycloalkyl ethers
  • C08B11/04—Alkyl or cycloalkyl ethers with substituted hydrocarbon radicals
  • C08B11/08—Alkyl or cycloalkyl ethers with substituted hydrocarbon radicals with hydroxylated hydrocarbon radicals; Esters, ethers, or acetals thereof
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
  • C08B15/00—Preparation of other cellulose derivatives or modified cellulose, e.g. complexes
  • C08B15/10—Crosslinking of cellulose
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K3/00—Use of inorganic substances as compounding ingredients
  • C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
  • C08K3/20—Oxides; Hydroxides
  • C08K3/22—Oxides; Hydroxides of metals
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/04—Oxygen-containing compounds
  • C08K5/07—Aldehydes; Ketones
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K7/00—Use of ingredients characterised by shape
  • C08K7/16—Solid spheres
  • C08K7/18—Solid spheres inorganic
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L1/00—Compositions of cellulose, modified cellulose or cellulose derivatives
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L1/00—Compositions of cellulose, modified cellulose or cellulose derivatives
  • C08L1/02—Cellulose; Modified cellulose

Definitions

• the present disclosure relates to a viscous composition and the like, and more particularly to a viscous composition containing cellulose nanocrystals.
• the contents of all documents described in this specification are incorporated herein by reference.
• Polymer thickeners are widely used for preparing viscous compositions in various fields, such as cosmetics and food fields.
• inorganic oxide particles may be mixed with a viscous composition and used as a sunscreen or the like.
• the thickening effect of the polymer thickener may be reduced by the inorganic oxide particles.
• the composition containing the polymer thickener and the inorganic oxide particles may have poor stability.
• hydroxyethyl cellulose (HEC) is also a component widely used as a polymer thickener, but since the thickening effect is reduced by the inorganic oxide particles, it is excellent while containing hydroxyethyl cellulose and inorganic oxide particles. It has not been easy to prepare a viscous composition having a high viscosity and stability.
• the present inventors have studied to find a novel means for providing a viscous composition containing hydroxyethyl cellulose and inorganic oxide particles but having excellent viscosity and stability.
• the present inventors have made a viscous composition obtained by mixing nanocellulose, particularly cellulose nanocrystal, with hydroxyethyl cellulose and dissolving it in water, and the viscosity does not easily decrease even when inorganic oxide particles are added, and the viscosity is stable. It was found to be a composition, and further studies were conducted.
• Item 1 Contains cellulose nanocrystals, hydroxyethyl cellulose, inorganic oxide particles, as well as water, The magnitude relationship between the storage elastic modulus G'and the loss elastic modulus G'' obtained by the frequency dispersion measurement is the storage elastic modulus G'> the loss elastic modulus G'> in the entire frequency range of 0.1 rad / s to 100 rad / s.
• Is Viscous composition.
• Item 2. Contains cellulose nanocrystals, hydroxyethyl cellulose, inorganic oxide particles, as well as water, The viscosity at 25 ° C. is 10,000 mPa ⁇ s or more. Viscous composition.
• the magnitude relationship between the storage elastic modulus G'and the loss elastic modulus G'' obtained by the frequency dispersion measurement is the storage elastic modulus G'> the loss elastic modulus G'> in the entire frequency range of 0.1 rad / s to 100 rad / s.
• Item 2. The viscous composition according to Item 2.
• Item 4. The viscous composition according to any one of Items 1 to 3, wherein the hydroxyethyl cellulose is hydroxyethyl cellulose crosslinked with a cross-linking agent.
• Item 5. Hydroxyethyl cellulose crosslinked with the crosslinking agent A crosslinked hydroxyethyl cellulose containing 0.35% by mass or more of a crosslinking agent.
• Item 4. The viscous composition according to Item 4.
• Item 6. The viscous composition according to Item 4 or 5, wherein the cross-linking agent is a dialdehyde compound.
• Item 7. Item 6. The viscous composition according to any one of Items 1 to 6, wherein the inorganic oxide is at least one selected from the group consisting of zinc oxide and titanium oxide.
• Item 8. Item 2. The viscous composition according to any one of Items 1 to 7, wherein the content of the inorganic oxide particles is 10% by mass or more.
• Item 9. Item 6. The viscous composition according to any one of Items 1 to 8, which is a composition for spraying.
• a method for producing a viscous composition which comprises mixing (1) a mixture of cellulose nanocrystals and hydroxyethyl cellulose with water, and (2) further adding inorganic oxide particles to the mixture.
• Item 11. (1) A method for producing a viscous composition for adding inorganic oxide particles, which comprises mixing a mixture of cellulose nanocrystals and hydroxyethyl cellulose with water.
• Item 12. Item 10. The method according to Item 10 or 11, further comprising mixing (0) cellulose nanocrystals and hydroxyethyl cellulose before (1).
• a viscous composition having excellent viscosity and stability while containing hydroxyethyl cellulose and inorganic oxide particles.
• the present disclosure preferably includes, but is not limited to, a viscous composition, a method for producing the same, and the like, and the present disclosure includes all disclosed in the present specification and recognized by those skilled in the art.
• the viscous composition included in the present disclosure contains cellulose nanocrystals, hydroxyethyl cellulose, inorganic oxide particles, and water.
• the viscous composition included in the present disclosure may be referred to as "the composition of the present disclosure”.
• Cellulose nanocrystal is a kind of nanocellulose.
• examples of nanocellulose made from wood or the like include cellulose nanofibers (CNF) and cellulose nanocrystals (CNC).
• CNF cellulose nanofibers
• CNC cellulose nanocrystals
• nanocellulose having a length of about 5 to 10 ⁇ m or more is often referred to as cellulose nanofiber (CNF)
• CNC cellulose nanocrystal
• the nanocrystalline cellulose described in Patent Document 1 Japanese Patent Laid-Open No. 2012-531478 can be preferably used.
• Cellulose is a natural polymer material that constitutes woody biomass and agricultural biomass together with hemicellulose and lignin. It is a homopolymer of repeating units of glucose linked by ⁇ -1,4-glycosidic bonds. Cellulose is formed linearly by ⁇ -1,4-glycosidic bonds, and they interact strongly with each other through hydrogen bonds. Due to its regular structure and strong hydrogen bonds, the cellulose polymer is highly crystalline and aggregates to form partial structures and microfibrils. Then, the microfibrils aggregate to form cellulosic fibers.
• Nanocellulose is a rod-shaped fibril with a length / diameter ratio of approximately 20-200.
• nanocellulose can be prepared, for example, from chemical pulp of wood fiber or agricultural fiber by removing the amorphous region mainly by acid hydrolysis to produce nano-sized fibril.
• Cellulose nanocrystals can be formed and stabilized in an aqueous suspension by, for example, sonicating the fibrils or passing them through a high shear microfluidizer.
• the second method is mainly physical processing. Bundles of microfibrils, usually tens of nanometers (nm) to several micrometer ( ⁇ m) in diameter, called cellulose microfibrils or microfibrillated cellulose, are produced by using high pressure homogenization and grinding. .. Steps with high intensity sonication have also been used to isolate fibril from natural cellulose fibers. High-intensity ultrasound can generate very strong mechanical vibration forces, which allows the separation of cellulose fibrils from biomass. This method produces microfibrillated cellulose having a diameter of less than about 60 nm, more preferably about 4 nm to about 15 nm, and a length of less than 1000 nm. Microfibrillated cellulose can also be subjected to, for example, further chemical, enzymatic and / or mechanical treatments. The microfibrillated cellulose can also be used as a cellulose nanocrystal.
• the cellulose nanocrystals used in the compositions of the present disclosure are, for example, by removing amorphous regions from pulp by acid hydrolysis, or by physical treatment such as high pressure treatment, pulverization treatment, and ultrasonic treatment. It can be appropriately prepared by treatment (and even by using these in combination).
• the cellulose portion of the cellulose nanocrystal used in the composition of the present disclosure may be a cellulose sulfate (cellulose sulfate).
• a sodium salt is preferable. That is, the cellulose portion of the cellulose nanocrystal used in the composition of the present disclosure may be cellulose sulfate sodium sulfate.
• cellulose nanocrystal indicates a crystal of nano-sized cellulose
• the cellulose may be an unmodified form or a modified form.
• the cellulose modified product for example, cellulose sulfate (particularly sodium cellulose sulfate) is preferably mentioned.
• examples of the CNC include nanocellulose having a thickness of about 1 to 100 nm and a length of about 50 to 500 nm.
• the upper or lower limit of the thickness range (1 to 100 nm) is, for example, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, and so on.
• the thickness range may be 2 to 99 nm.
• the upper limit or the lower limit of the length range (50 to 500 nm) is, for example, 60, 70, 80, 90, 100, 110, 120, 130, 140, 150, 160, 170, 180, 190, 200, 210. , 220, 230, 240, 250, 260, 270, 280, 290, 300, 310, 320, 330, 340, 350, 360, 370, 380, 390, 400, 410, 420, 430, 440, 450, 460. It may be 470, 480, or 490 nm.
• the length range may be 60 to 490 nm.
• the ratio (length / thickness) of the length (nm) to the thickness (nm) can be, for example, about 1 to 200.
• the upper or lower limit of the range of the ratio is, for example, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21. , 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46. , 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71.
• the hydroxyethyl cellulose (HEC) used in the composition of the present disclosure is not particularly limited as long as the effect is not impaired.
• hydroxyethyl cellulose not cross-linked with a cross-linking agent can be preferably used as the HEC of the composition of the present disclosure.
• Cross-linked HEC is more preferred.
• the cross-linking agent include polyvalent aldehyde compounds (preferably dialdehyde compounds) such as glutaraldehyde and glioxal, 2,2-bishydroxymethylbutanol-tris [3- (1-aziridinyl) propionate], 1,8-.
• polyvalent aziridin compounds such as hexamethylene diethylene urea
• polyvalent isocyanate compounds such as tolylene diisocyanate and hexamethylene diisocyanate.
• dialdehyde compounds are preferred, and glyoxal is particularly preferred.
• the cross-linking agent may be used alone or in combination of two or more.
• the cross-linked HEC preferably has a cross-linking agent content of, for example, 0.05% by mass or more, and more preferably about 0.05 to 2% by mass.
• the upper or lower limit of the cross-linking agent content ratio range is, for example, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.11, 0.12, 0.13, 0.14, 0.15, 0.16, 0.17, 0.18, 0.19, 0.2, 0.21, 0.22, 0.23, 0.24, 0.25, 0.
• the cross-linking agent content ratio range may be 0.1 to 1% by mass. In particular, 0.35% by mass or more is preferable.
• Cross-linking of hydroxyethyl cellulose with a cross-linking agent can be carried out by a known method or a method that can be easily conceived from a known method. For example, it can be carried out by the method described in Japanese Patent Publication No. 58-43402.
• the HEC (including non-crosslinked HEC and crosslinked HEC) preferably has a viscosity of a 1.33% by mass (w / w%) aqueous solution at 25 ° C. of 4000 mPa ⁇ s or more, and more preferably 4000 to 18000 mPa ⁇ s. preferable.
• the upper or lower limit of the viscosity range is, for example, 4100, 4200, 4300, 4400, 4500, 4600, 4700, 4800, 4900, 5000, 5100, 5200, 5300, 5400, 5500, 5600, 5700, 5800, 5900, 6000.
• the viscosity range may be 4100 to 17900 mPa ⁇ s.
• the HEC (including the non-crosslinked HEC and the crosslinked HEC) is not particularly limited, but the molecular weight is preferably, for example, about 1800000 to 430000.
• the upper or lower limit of the molecular weight range is, for example, 19000000, 2000000, 210000, 2200, 230000, 2400000, 25, 260000, 2700, 280000, 2900, 3000, 3100, 3200, 3300, 3400, 3500, 3600, 3700, 380000, It may be 3900000, 4000, 410000, or 4200000.
• the molecular weight range may be 1900000 to 4200000.
• the molecular weight is a mass average molecular weight obtained by gel permeation chromatography (GPC) and converted into polyethylene oxide.
• GPC gel permeation chromatography
• Examples of the column for measuring the mass average molecular weight in terms of polyethylene glycol by GPC include Shodex OHpak SB-807HQ, Shodex OHpak SB-806HQ, Shodex OHpak SB-804HQ and the like. Detailed GPC measurement conditions are shown below.
• HEC is a compound in which the OH group of cellulose is OR (R indicates H or CH 2 CH 2 OH), and is contained in the composition of the present disclosure.
• R indicates H or CH 2 CH 2 OH
• a group other than H or CH 2 CH 2 OH may be present as R of the OR, but it is preferable that no hydrophobic group is present as R.
• R an alkyl group, particularly a linear chain having 6 to 20 carbon atoms (6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20) or Those having a branched chain alkyl group (more specifically, for example, a cetyl group) may be used, but it is preferable not to use them.
• the composition of the present disclosure contains water as a solvent. Further, a solvent other than water may be further contained as long as the effect of the composition of the present disclosure is not impaired.
• the solvent other than water include water-soluble solvents, and for example, water-soluble organic solvents are preferable.
• the water-soluble organic solvent include monohydric or divalent alkyl alcohols having 1 to 6 carbon atoms (1, 2, 3, 4, 5, or 6), and more specifically, for example. Examples thereof include ethanol and butylene glycol.
• the value of the storage elastic modulus (G') is larger than the value of the loss elastic modulus (G'') (that is, the storage elastic modulus G'> the loss elastic modulus G'').
• the composition of the present disclosure preferably has a loss tangent (tan ⁇ ) of less than 1 (that is, tan ⁇ ⁇ 1).
• the loss tangent (tan ⁇ ) is the ratio (G ′′ / G ′) of the storage elastic modulus (G ′) and the loss elastic modulus (G ′′), and is used as one of the indexes of the viscoelastic property.
• the larger the value of the loss tangent the smaller the elastic modulus.
• the loss tangent is used as an index of sol and gel, and usually tan ⁇ > 1 is sol and tan ⁇ ⁇ 1 is gel.
• the values of the storage elastic modulus G ′ and the loss elastic modulus G ′′ can be measured at 25 ° C. using a viscoelasticity measuring device (leometer). More specifically, after confirming the linear region by measuring the strain dispersion at 1 Hz, an appropriate distortion is selected within the range of the linear region, and the frequency dispersion at 25 ° C. (frequency: 0.1 rad / s to 100 rad / s). And observe the magnitude relationship between G'and G''.
• the storage elastic modulus G'and the loss elastic modulus G'' obtained by frequency dispersion measurement have a magnitude relationship of the storage elastic modulus G in the entire range of frequency: 0.1 rad / s to 100 rad / s. It is preferable that'> loss elastic modulus G''.
• composition of the present disclosure has a viscosity at 25 ° C. of 10,000 mPa ⁇ s or more, preferably 10,000 to 35,000 mPa ⁇ s.
• the upper or lower limit of the viscosity range is, for example, 10100, 10200, 10300, 10400, 10500, 10600, 10700, 10800, 10900, 11000, 11100, 11200, 11300, 11400, 11500, 11600, 11700, 11800, 11900, 12000.
• the viscosity is a value measured at 25 ° C. using a rotary viscometer manufactured by BrookField (model number: DVE, spindle: LV) at a rotation speed of 20 rpm.
• the spindle used for measurement is spindle LV-1 when it is less than 200 mPa ⁇ s, spindle LV-2 when it is 200 mPa ⁇ s or more and less than 1000 mPa ⁇ s, and 1000 mPa ⁇ s or more and less than 4000 mPa ⁇ s.
• the inorganic oxide particles are preferably known inorganic oxide particles used as a sunscreen component, and more specifically, they are selected from the group consisting of, for example, cerium oxide, iron oxide, talc, zinc oxide and titanium oxide. It is preferably at least one kind of particles to be formed.
• inorganic oxide particles for example, inorganic oxide powder can be used.
• the inorganic oxide particles may be treated with hydrophilicity. Examples of the hydrophilic treatment include hydrogen dimethicone treatment, aluminum oxide or aluminum hydroxide treatment, and fatty acid (particularly stearic acid) treatment. The hydrophilic treatment is preferably applied to the surface of the particles. Further, the inorganic oxide particles may be used alone or in combination of two or more.
• CNC is preferably about 0.05 to 1 part by mass.
• the upper or lower limit of the range is, for example, 0.1, 0.15, 0.2, 0.25, 0.3, 0.35, 0.4, 0.45, 0.5, 0.55, It may be 0.6, 0.65, 0.7, 0.75, 0.8, 0.85, 0.9, or 0.95.
• the range may be 0.1 to 0.8.
• the CNC content in the composition of the present disclosure is not particularly limited as long as the effect is not impaired, and examples thereof include about 0.1 to 5% by mass.
• the upper or lower limit of the range is, for example, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1, 1.1, 1.2.
• the HEC (including non-crosslinked HEC and crosslinked HEC) content in the composition of the present disclosure is not particularly limited as long as the effect is not impaired, but is, for example, about 0.1 to 5% by mass. Can be mentioned.
• the upper or lower limit of the range is, for example, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1, 1.1, 1.2.
• the content of the inorganic oxide particles in the composition of the present disclosure is preferably 10% by mass or more, more preferably about 10 to 30% by mass.
• the upper or lower limit of the range (10 to 30% by mass) is, for example, 10.1, 10.2, 10.3, 10.4, 10.5, 10.6, 10.7, 10.8, 10. 9, 10, 11.1, 11.2, 11.3, 11.4, 11.5, 11.6, 11.7, 11.8, 11.9, 12, 12.1, 12.2, 12.3, 12.4, 12.5, 12.6, 12.7, 12.8, 12.9, 13, 13.1, 13.2, 13.3, 13.4, 13.5, 13.6, 13.7, 13.8, 13.9, 14, 14.1, 14.2, 14.3, 14.4, 14.5, 14.6, 14.7, 14.8, 14.9, 15, 15.1, 15.2, 15.3, 15.4, 15.5, 15.6, 15.7, 15.8, 15.9, 16, 16.1, 16.
• the composition of the present disclosure can stably contain inorganic oxide particles. Therefore, in the composition of the present disclosure, the separation and / or aggregation of the inorganic oxide particles is preferably suppressed. More specifically, for example, the composition of the present disclosure preferably suppresses separation and / or aggregation of inorganic oxide particles even when stored at 50 ° C. for 10 days immediately after production.
• composition of the present disclosure may contain components other than CNC, HEC (including non-crosslinked HEC and crosslinked HEC), inorganic oxide particles, and water as long as the effect is not impaired.
• HEC including non-crosslinked HEC and crosslinked HEC
• inorganic oxide particles and water as long as the effect is not impaired.
• examples of such an ingredient include simple substances and ingredients known in the fields of pharmaceuticals, cosmetics, and foods.
• composition of the present disclosure can be prepared, for example, by mixing CNC and HEC (including non-crosslinked HEC and crosslinked HEC) and then mixing the mixture with water. Thus, it is desirable to mix CNC and HEC before adding to water.
• both CNC and HEC used for mixing before being added to water are powders. Further, the mixture of CNC and HEC to be added to water is preferably a powder.
• composition of the present disclosure can be prepared, for example, by adding inorganic oxide particles to a viscous composition prepared by adding a mixture of CNC and HEC to water and mixing them as necessary.
• a viscous composition prepared by adding a mixture of CNC and HEC to water and mixing them as necessary is useful as a viscous composition for adding inorganic oxide particles.
• composition of the present disclosure can be preferably placed in a spray container and sprayed smoothly. Since it is a viscous composition that can be sprayed while containing inorganic oxide particles, it can be preferably used as a composition for spraying. Such compositions are particularly suitable for application to the skin as sunscreens and the like. When the composition of the present disclosure is used by spraying, it is preferable to use it by filling it in, for example, a manual spray.
• composition of the present disclosure has excellent viscosity and viscoelasticity, it is useful in technical fields in which products required to have such properties exist, for example, in the fields of pharmaceuticals, cosmetics, and foods. That is, the composition of the present disclosure can be preferably used, for example, as a pharmaceutical composition, a cosmetic composition, a food composition, or the like.
• Measurement conditions Leometer: TA Instrument AR-2000ex Plate: 60 mm, 1 ° cone plate Measurement temperature: 25 ° C Distortion: 0.1 to 10% (selected within the range of the linear region obtained in the distortion dispersion measurement at 1 Hz) Frequency: 0.1 rad / s to 100 rad / s
• Viscosity measurement The viscosity of each viscous composition was measured at 25 ° C. using a rotary viscometer (model number: DVE, spindle: LV) manufactured by BrookField at a rotation speed of 20 rpm.
• the spindle used for measurement is spindle LV-1 when it is less than 200 mPa ⁇ s, spindle LV-2 when it is 200 mPa ⁇ s or more and less than 1000 mPa ⁇ s, and 1000 mPa ⁇ s or more and less than 4000 mPa ⁇ s.
• HEC water-soluble polymers
• All powders were purchased and used.
• HEC (CF-Y) is manufactured by Sumitomo Seika Co., Ltd.
• the HEC (CF-Y) used is a cross-linked HEC cross-linked with a cross-linking agent (glyoxal), and the cross-linking agent content is 0.55% by mass.
• Zinc oxide (FINEX-33W: Sakai Chemical Industry Co., Ltd.) and titanium oxide (MT-100TV: TAYCA Corporation) were used as the inorganic oxides.
• the zinc oxide has been treated with a hydrogen dimethicone, and the titanium oxide has been treated with aluminum oxide or aluminum hydroxide and stearic acid.
• a powder of crystal nanocellulose and a powder of a water-soluble polymer are mixed, and the mixed powder is stirred and mixed with ion-exchanged water to dissolve it, and further an inorganic oxide is added thereto.
• HEC or carbomer water-soluble polymer
• Zinc oxide or titanium oxide was mixed to prepare a viscous composition. More specifically, 0.33 g of cellulose nanocrystal and 1 g of hydroxyethyl cellulose or carbomer are mixed in a powder state, the mixed powder is put into water, and the mixture is stirred with a 4-sheet paddle stirring blade at 550 rpm for 4 hours to gel. I made it.

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• 2021
  • 2021-09-30 JP JP2022554087A patent/JPWO2022071473A1/ja active Pending
  • 2021-09-30 WO PCT/JP2021/036061 patent/WO2022071473A1/ja not_active Ceased

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